DRE VENTURA— 510(k) K132903

Name: FDA 510(k) clearance K132903
Creator: U.S. Food and Drug Administration
Published: 2014-07-01

Substantially Equivalent

Dre Medical, Inc.

FDA 510(k) clearance K132903 for DRE VENTURA, Substantially Equivalent on 2014-07-01. Applicant: Dre Medical, Inc.. Device class: 2.

Clearance details

Applicant: Dre Medical, Inc.
Product code: Code BSZ
Device class: Class 2
Regulation: 21 CFR 868.5160
Advisory panel: Anesthesiology
Date received: 2013-09-16
Decision date: 2014-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Louisville, KY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code BSZ

product code BSZ

Death: 23
Injury: 298
Malfunction: 32,987
Total: 33,308

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.